A Compliance Ready Solution for Small to Medium Medical Device Organizations

Data Sheet:
A Compliance Ready Solution for Small to Medium Medical Device Organizations

Complying with FDA, EU and other regulations is a fact of life for medical device manufacturers and suppliers, irrespective of size or market sector. The burden of
meeting these requirements is often most acutely felt in small to medium sized organizations (SMEs) that do not have the resources to implement the type of enterprise label lifecycle management solution that can automate much of the compliance process and reduce the load.Software-as-a-Service model enables SME medical device manufacturers to achieve rapid compliance and end-to-end label lifecycle management.

PRISYM ID - SAP Datasheet

Download Form